New Staph-Fighting skin regimen shows promise in High-Risk community

NCT ID NCT06210594

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a combination of topical antibiotics and antiseptic washes could reduce staph bacteria on the skin of Native American adults living on or near tribal lands. Participants were at high risk for staph infections due to diabetes, obesity, or recent infections. The trial compared the biomedical regimen plus education and household supplies to education and supplies alone, measuring staph carriage and infection rates.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Mupirocin (Bactroban) + Nozin + chlorhexidine gluconate (Hibiclens)
What this could lead to
If successful, this approach could reduce staph infections in high-risk communities by lowering the amount of staph bacteria on the skin.
What could go wrong
This is a small, completed Phase 4 trial with only 78 participants, so results may not apply to broader populations. The regimen requires ongoing use, and long-term adherence may be challenging.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

78 people

The number who actually took part.

Started

Apr 2024

Finished

Nov 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Native American adult living on or adjacent to the WMA Tribal lands * 18 years of age and older * Lab-confirmed SA carriage at time of enrollment * Ability to provide written informed consent * Ability to comply with follow-up activities * Risk factor for SA-associated infection: Diagnosed with diabetes OR body mass index ≥30 OR documented SSTI or SA infection in the past 3 years Exclusion Criteria: * Immediate family member of study staff * Allergy to citrus or any ingredient in Nozin, Hibiclens, or mupirocin * Without a permanent home (e.g., living in a group home, shelter, or is unhoused) * Use of antibiotics within 30 days prior to the first study visit (time-limited) * Current SA infection (time-limited)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Whiteriver Center for Indigenous Health

    Whiteriver, Arizona, 85941, United States

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